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临床试验/NCT05467631
NCT05467631已完成不适用

Topical Phytoterpene Mixture for Treatment of Plantar Fasciitis in Adults

Center for Biomedical Research, Inc.2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2019年1月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
2
主要终点
Change in Pain Score Between Baseline and 2 Weeks

研究概览

简要总结

Randomized controlled trial of mixture of essential oils containing tea tree oil, rosemary, clove, pepper, in a formulation with skin permeation enhancers including limonene for the treatment of plantar fasciitis in adult men and women. Forty-two patients will be randomized to receive twice daily topical application of the treatment formulation or plain tea tree oil as a control. Analog pain scores will be assessed at the start of treatment and at two weeks. Analysis will be by student's T-test.

详细描述

Randomized controlled trial of mixture of essential oils containing tea tree oil, rosemary, clove, pepper, in a formulation with skin permeation enhancers including limonene for the treatment of plantar fasciitis in adult men and women. Forty-two patients will be randomized to receive twice daily topical application of the treatment formulation or plain tea tree oil as a control. Analog pain scores will be assessed at the start of treatment and at two weeks. Analysis will be by student's T-test. Primary outcome measure will be the difference in pain score between baseline score and pain score at 2 weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

Identical bottles given to participants with serial number, aroma and feel of each treatment group is the same

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Plantar fasciitis diagnosed by a medical practitioner and at least 3 months in duration

排除标准

  • Age under 18 years, any history of diabetes, history of foot surgery

结局指标

主要结局

Change in Pain Score Between Baseline and 2 Weeks

时间窗: 2 weeks

Patients will be asked to rate pain on a 1-10 analog scale at the start of the study and at 2 weeks

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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